1. Volume 107, Issue 5, Pages 617-629 (November 2001)
Forebrain-Specific Calcineurin Knockout Selectively Impairs Bidirectional Synaptic Plasticity and Working/Episodic-like Memory 
Hongkui Zeng, Sumantra Chattarji, Michaela Barbarosie, Laure Rondi-Reig, Benjamin D. Philpot, Tsuyoshi Miyakawa, Mark F. Bear, Susumu Tonegawa 
Cell 
Volume 107, Issue 5, Pages (November 2001)
DOI: /S (01)

2. Figure 1
The Generation of Forebrain-Specific Calcineurin Knockout Mice
(A) Schematic diagram of the procedure for generating the fCNB1 ES clones. (Top) Wild-type CNB1 locus. Exons are labeled as E1–E5 in which coding regions are indicated as filled boxes. (Middle) Targeting vector in which a loxP site was inserted in intron 1, a LFNT cassette was inserted in intron 4, and a diphtheria toxin (DT-A) marker was inserted at the 3′ end. (Bottom) Floxed CNB1 locus. Restriction enzymes abbreviations are as follows: RI, EcoRI; Pm, PmeI; Pa, PacI; Ba, BamHI; Xh, XhoI; and RV, EcoRV.
(B) In situ hybridization using a CNB1 probe to demonstrate the Cre-mediated CNB1 gene deletion pattern. Whole brain sections from mice of 4 months of age include sagital sections (top and middle) and coronal sections (bottom). Bright-field images are shown in which silver grains representing mRNA signals are in black and hematoxylin counterstaining is in blue. Abbreviations are as follows: CTX, cortex; H, hippocampus; S, striatum; TH, thalamus; CB, cerebellum; A, amygdala; and P, piriform cortex.
(C) Ontogeny of Cre-mediated CNB1 deletion in the hippocampus. Sections from mutant mice with various ages are shown along with a section from a control mouse of 4 months of age.
Cell  , DOI: ( /S (01) )

3. Figure 2
Immunohistochemical Staining with Anti-CNB and Anti-CNA Antibodies
(A) Coronal sections from mice of 5 months of age showing the general distributions of CNB and CNA proteins double-stained with anti-CNB and anti-CNA simultaneously. CNB and CNA proteins exhibit identical patterns in either control (top) or mutant (bottom) sections. In the mutant sections, both proteins are missing in selected cell types of the hippocampus, cortex, and amygdala. Immunostaining of another group of mice of 12 weeks of age exhibited similar patterns (data not shown).
(B) Higher magnification images of the hippocampal subfields showing the loss of CNA protein in CA1 pyramidal cells and dentate gyrus (DG) granule cells but not CA3 pyramidal cells. Abbreviations are as follows: s.p., stratum pyramidale; s.r., stratum radiatum; s.o., stratum oriens; s.l., stratum lucidum; and s.g., stratum granulosum.
Cell  , DOI: ( /S (01) )

4. Figure 3
Impaired LTD and Frequency-Dependent Bidirectional Synaptic Plasticity, But Normal 100 Hz LTP and Depotentiation in Schaffer Collateral-CA1 Synapse
Filled circles indicate CN-KO data, and open circles indicate control data.
(A) Stimulation (1 Hz) induced normal LTD in control slices but significantly diminished LTD in mutant slices.
(B) Stimulation (10 Hz) induced modest potentiation in the mutant slices.
(C) Stimulation (40 Hz) induced enhanced LTP in the mutant slices.
(D) Control and mutant slices showed no difference in LTP induced by 1 tetanus of 100 Hz.
(E) Summary of the fEPSP changes with different stimulation frequencies.
(F1) Following TBS-induced LTP, LFS given at 30 min post-TBS elicits depotentiation of comparable magnitude in both mutant and control slices.
(F2) Data presented in (F1) were replotted by renormalizing to baseline the potentiated fEPSPs from the final 10 min of LTP prior to delivery of LFS.
(G) Paired-pulse facilitation was not altered in the mutant slices across all interstimulus intervals.
Cell  , DOI: ( /S (01) )

5. Figure 4
Deletion of Calcineurin Does Not Alter NMDA Receptor Current Properties
(A) I-V curve of normalized NMDA currents from control (open circles) and mutant (closed circles) cells. Voltage was adjusted by the measured junction potential, and currents were normalized to the response at +44 mV.
(B) Scatter plot with mean and SEM of the weighted time constant (τw) of the NMDAR EPSC decay. Traces depict normalized NMDAR EPSC from control (1) and mutant (2) mice, as well as an overlay of the two (1 + 2).
(C) Average temporal summation of NMDAR EPSCs to 40 Hz stimulation. Currents were normalized to the peak response evoked by the first pulse. Inset depicts a sample trace, and dashed lines demonstrate how total amplitude was measured for each pulse.
Cell  , DOI: ( /S (01) )

6. Figure 5 Normal Contextual and Cued Fear Conditioning
(A) Freezing responses after training with three tone-shock pairs. Pretrain indicates the freezing levels in Box A (the shocking chamber) before the onset of training. Context indicates the freezing levels in Box A after training. Pretone indicates the freezing levels in Box B after training and before the tone testing. Tone indicates the freezing levels in Box B during the presentation of tone.
(B) Freezing responses in Box A during the extinction test following the tests for contextual and cued fear shown in (A). Training was given on day 1. Context test was done on day 2. Tone test was done on day 3. Context extinction test was subsequently done from day 4 to day 7.
Cell  , DOI: ( /S (01) )

7. Figure 6 The Hidden Platform Morris Water Maze Task
(A) The 10 day spatial reference memory training plus 5 day reversal training. Escape latencies were averages of four trials for each day. Escape latencies of all three types of controls were shown separately to demonstrate that there was no significant difference among them. Subsequently they were pooled as one single control group. Closed circles indicate mutants, open circles indicate homozygous fCNB1 control, open triangles indicate CW2-Cre control, and open squares indicate wild-type control.
B) Swimming speeds averaged from all trials on days 10 and 11.
(C) Percentage of time spent in the peripheral area of the maze, i.e., a 15-cm-wide zonal area adjacent to the wall. The data presented are averages from all trials on days 10 and 11.
(D) Probe test on day 10, after the first-platform training. Left graph shows the quadrant occupancy. Right graph shows the number of crossings at the original platform location. (E) Probe test on day 15, after the second-platform training. Left graph shows the quadrant occupancy. Right graph shows the number of crossings at the new platform location. Abbreviations are as follows: TA, target quadrant; AL, adjacent left quadrant; AR, adjacent right quadrant; and OP, opposite quadrant. Dotted lines in all probe tests depict chance level (15 s) in random searching.
Cell  , DOI: ( /S (01) )

8. Figure 7 Delayed Matching-to-Place Task
(A) Latencies of the first five trials of new platform training, averaged from the last two training sessions (the fifth and the sixth platform locations). See supplemental data for more data on all training sessions.
(B) The reduction of latencies (saving time) between the first and second trials of each session, averaged from the last two training sessions.
(C) Swimming speeds averaged from the first two trials of the last two training sessions.
Cell  , DOI: ( /S (01) )

9. Figure 8
Spatial Working Memory in the 8/8 Version of the 8 Arm Radial Maze
Data were presented as 2 day/trial averages.
(A) Total number of revisiting errors (i.e., working memory errors) across training.
(B) The number of different arms chosen in the first eight arm visits.
(C) Number of omission errors, i.e., arm was visited but food was not taken, as an indication of motivation.
(D) Each arm visit was categorized into one of the five groups according to the angle shift between this arm and the previously visited arm, and the percentage of arm visits contained in each group was shown. This plot is intended to reveal if the animal has taken a serial (nonspatial) search strategy, in which case there would be a high percentage of 45° shift. The data were averages from the last four trials.
(E) Running speed across training.
Cell  , DOI: ( /S (01) )